Canonical Allele Identifier: PA1139748379
Gene: SLC52A3 HGNC NCBI

Linked Data

ClinVar Variation Id: 929978

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_212134.3:p.Met317Ile
CA310677077
NM_033409.4:c.951G>A
CA407962760
NM_033409.4:c.951G>T
CA407962761
NM_033409.4:c.951G>C